SCHEMBL304931

SCHEMBL304931

BrC1(c2ccccc2)c2ccccc2-c2ccccc21

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CFTR P13569 1/20 0.42
GOPC Q9HD26 1/20 0.42
THRB P10828 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
SMN1; SMN2 Q16637 3/20 0.40
LMNA P02545 2/20 0.40
MAPT P10636 2/20 0.40
S100A4 P26447 1/20 0.40
KDM4E B2RXH2 1/20 0.40
MEN1 O00255 1/20 0.40
OPRK1 P41145 1/20 0.40
KMT2A Q03164 1/20 0.40
CYP19A1 P11511 2/20 0.39
CYP2D6 P10635 1/20 0.38
PDK2 Q15119 1/20 0.38
APEX1 P27695 1/20 0.36
NPC1 O15118 1/20 0.36
POLB P06746 1/20 0.36
NPSR1 Q6W5P4 2/20 0.35
GAA P10253 2/20 0.35

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL29769743 1.00 CFTR (0.42) CFTRGOPCTHRBTDP1SMN1; SMN2
SCHEMBL11453348 0.87 ALDH1A1 (0.40) CFTRGOPCTDP1LMNAOPRK1
SCHEMBL11453227 0.87 CFTR (0.46) CFTRGOPCTHRBSMN1; SMN2LMNA
SCHEMBL24279299 0.83 PDK2 (0.53) CFTRGOPCSMN1; SMN2LMNAMAPT
SCHEMBL31003499 0.78 PDK2 (0.42) LMNAOPRK1PDK2NPSR1
SCHEMBL23630503 0.76 DNMT1 (0.38) CFTRGOPCTHRBTDP1SMN1; SMN2
SCHEMBL7031351 0.75 ALOX5 (0.38) CFTRGOPCLMNAMEN1KMT2A
SCHEMBL6856706 0.74 CFTR (0.45) CFTRGOPCTHRBTDP1SMN1; SMN2
SCHEMBL129053 0.74 MEN1 (0.67) CFTRGOPCTHRBTDP1SMN1; SMN2
SCHEMBL29392072 0.74 MEN1 (0.67) CFTRGOPCTHRBTDP1SMN1; SMN2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 406 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117623959-A Synthesis method of threo-3-fluoro-N-9-phenyl-9-fluorene-L-tert-butyl aspartate 吉尔多肽生物制药(大连市)有限公司 2024-03-01 CN claimed
CN-113861403-B Nanometer material and preparation method and application thereof 北京化工大学 2024-01-26 CN claimed
CN-104603215-A Composition for coating high refractive layer and transparent conductive film comprising same LG HAUSYS LTD 2015-05-06 CN claimed
US-6797745-B1 Hot melt inks containing styrene or terpene polymers XEROX CORPORATION 2004-09-28 US claimed
US-20260070945-A1 MACROCYCLIC IMMUNOMODULATORS BRISTOL-MYERS SQUIBB COMPANY 2026-03-12 US disclosed
US-20260022142-A1 MACROCYCLIC IMMUNOMODULATORS BRISTOL MYERS SQUIBB CO (US) 2026-01-22 US disclosed
EP-4644366-A1 PREPARATION METHODS FOR PILOCARPINE AND INTERMEDIATE COMPOUND THEREOF Zhejiang Ausun Pharmaceutical Co., Ltd. (CN) 2025-11-05 EP disclosed
US-20250289830-A1 KRAS INHIBITORS ELI LILLY AND COMPANY 2025-09-18 US disclosed
US-20250250299-A1 MACROCYCLIC IMMUNOMODULATORS BRISTOL-MYERS SQUIBB COMPANY 2025-08-07 US disclosed
US-12351591-B2 KRas inhibitors ELI LILLY AND COMPANY (US) 2025-07-08 US disclosed
CN-118909031-B Anti-coronavirus compounds, compositions and uses thereof 上海柯君医药科技有限公司 2025-05-27 CN disclosed
US-20250163104-A1 MACROCYCLIC IMMUNOMODULATORS BRISTOL MYERS SQUIBB CO (US) 2025-05-22 US disclosed
US-5571825-A Method of selectively inhibiting prostaglandin G/H synthase-2 WARNER-LAMBERT COMPANY (US) 1996-11-05 US disclosed
EP-0643710-A1 SYNTHESIS OF OPTICALLY ACTIVE LACTONES FROM L-ASPARTIC ACID AND INTERMEDIATES THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-03-22 EP disclosed
CN-1027695-C Heterocyclic-NMDA antagonists MERRELL DOW PHARMA (US) 1995-02-22 CN disclosed
CN-1098107-A modified oligodeoxynucleotides, their preparation and their therapeutic use SANKYO CO (JP) 1995-02-01 CN disclosed
EP-0611075-A1 Modified oligodeoxyribonucleotides, their preparation and their therapeutic use SANKYO COMPANY LIMITED (JP) 1994-08-17 EP disclosed
US-5322942-A Deprotecting and hydrolyzing protected aspartic acid diester, reacting with nitrosylating agent in presence of hydrogen halide, esterifying, reacting with acyl aryl derivative REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1994-06-21 US disclosed
WO-1992021675-A1 SYNTHESIS OF OPTICALLY ACTIVE LACTONES FROM L-ASPARTIC ACID AND INTERMEDIATES THEREOF THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1992-12-10 WO disclosed
CN-1056499-A HETEROCYCLIC-NMDA ANTAGONISTS MERRELL DOW PHARMA (US) 1991-11-27 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (6 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250163104-A1 MACROCYCLIC IMMUNOMODULATORS CD274, PDCD1LG2, PDCD1 CFTR 2714/4885GOPC 873/4885THRB 3623/4885
US-20260022142-A1 MACROCYCLIC IMMUNOMODULATORS CD274, PDCD1LG2, PDCD1 CFTR 1664/4885GOPC 266/4885THRB 2562/4885
US-20260070945-A1 MACROCYCLIC IMMUNOMODULATORS CD274, PDCD1, PDCD1LG2 CFTR 1808/4885GOPC 249/4885THRB 2734/4885
US-20250250299-A1 MACROCYCLIC IMMUNOMODULATORS CD274, PDCD1LG2, PDCD1 CFTR 2969/4885GOPC 749/4885THRB 3552/4885
US-12351591-B2 KRas inhibitors KRAS, NRAS, HRAS CFTR 53/4885GOPC 3163/4885THRB 1443/4885
US-20250289830-A1 KRAS INHIBITORS KRAS, NRAS, HRAS CFTR 53/4885GOPC 3163/4885THRB 1443/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.